Kataoka Hiroshi, Ida Takashi, Ishii Yoshikazu, Tateda Kazuhiro, Oguri Toyoko, Yoshida Atsushi, Okuzumi Katsuko, Oishi Tsuyoshi, Tsukahara Miyuki, Mori Shin-Ichiro, Yoneyama Akiko, Araoka Hideki, Mitsuda Toshihiro, Sumitomo Midori, Moriya Kyoji, Goto Mieko, Nakamori Yoshitaka, Shibayama Akiyoshi, Ohmagari Norio, Sato Tomoaki, Yamaguchi Keizo
Pharmaceutical Research Center, Meiji Seika Pharma Co., Ltd., Tokyo 104 8002, Japan.
Department of Microbiology and Infectious Diseases, Faculty of Medicine, Toho University School of Medicine, 5-21-16 Omori-nishi, Ota-ku, Tokyo 143 8540, Japan.
J Glob Antimicrob Resist. 2013 Jun;1(2):91-96. doi: 10.1016/j.jgar.2013.03.005. Epub 2013 Apr 23.
Infections caused by multidrug-resistant (MDR) Pseudomonas aeruginosa are very difficult to treat. The aim of this study was to develop more effective treatments by investigating in vitro the effects of combinations of antibiotics against 47 MDR P. aeruginosa isolates harbouring various resistance factors. The isolates included 41 (87%) metallo-β-lactamase (MBL)-positive strains, 37 (79%) strains with mutations in OprD and 46 (98%) strains carrying the genes encoding aminoglycoside-modifying enzymes (AMEs). The quinolone resistance-determining region was mutated in all of the strains. These strains were classified into 16 groups according to amplified fragment length polymorphism and resistance factors. The effects of combinations of antibiotics on 16 representative strains were determined using a 'Break-point Checkerboard Plate' assay. Combinations of amikacin+aztreonam (coverage rate, 81.3%) and arbekacin+aztreonam (93.8%) inhibited growth. In contrast, combinations of ciprofloxacin+meropenem (6.3%) and ciprofloxacin+ceftazidime (12.5%) were much less effective. Aztreonam and arbekacin (or amikacin) are not substrates for MBLs and AMEs, respectively. We conclude that the combined effects of these drugs were possibly because of resistance factors.
多重耐药铜绿假单胞菌引起的感染很难治疗。本研究的目的是通过体外研究抗生素组合对47株携带各种耐药因子的多重耐药铜绿假单胞菌分离株的影响,开发更有效的治疗方法。这些分离株包括41株(87%)金属β-内酰胺酶(MBL)阳性菌株、37株(79%)外膜孔蛋白D(OprD)发生突变的菌株和46株(98%)携带编码氨基糖苷修饰酶(AME)基因的菌株。所有菌株的喹诺酮耐药决定区均发生突变。根据扩增片段长度多态性和耐药因子,将这些菌株分为16组。使用“断点棋盘格平板”试验确定抗生素组合对16株代表性菌株的影响。阿米卡星+氨曲南组合(覆盖率81.3%)和阿贝卡星+氨曲南组合(93.8%)可抑制生长。相比之下,环丙沙星+美罗培南组合(6.3%)和环丙沙星+头孢他啶组合(12.5%)的效果要差得多。氨曲南和阿贝卡星(或阿米卡星)分别不是MBL和AME的作用底物。我们得出结论,这些药物的联合作用可能是由于耐药因子。